CL2009000089A1 - Processes for preparing a derivative of y-amino-o-biphenyl-x-methyl-pentanoic acid, intermediate compounds and their preparation process; use of the compounds in the synthesis of nep inhibitor compounds, useful in cardiovascular diseases, such as hypertension, congestive heart failure, among others. - Google Patents

Processes for preparing a derivative of y-amino-o-biphenyl-x-methyl-pentanoic acid, intermediate compounds and their preparation process; use of the compounds in the synthesis of nep inhibitor compounds, useful in cardiovascular diseases, such as hypertension, congestive heart failure, among others.

Info

Publication number
CL2009000089A1
CL2009000089A1 CL2009000089A CL2009000089A CL2009000089A1 CL 2009000089 A1 CL2009000089 A1 CL 2009000089A1 CL 2009000089 A CL2009000089 A CL 2009000089A CL 2009000089 A CL2009000089 A CL 2009000089A CL 2009000089 A1 CL2009000089 A1 CL 2009000089A1
Authority
CL
Chile
Prior art keywords
compounds
synthesis
biphenyl
amino
methyl
Prior art date
Application number
CL2009000089A
Other languages
Spanish (es)
Inventor
David Hook
Jonathan Medlock
Bernhard Riss
Philippe Polleux
Matthias Napp
Erhard Bappert
Daniel Kaufmann
Antonio Zanotti-Gerosa
Original Assignee
Novartis Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of CL2009000089A1 publication Critical patent/CL2009000089A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C269/00Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C269/06Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups by reactions not involving the formation of carbamate groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2632-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2632-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
    • C07D207/2672-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36Oxygen or sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/22Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from lactams, cyclic ketones or cyclic oximes, e.g. by reactions involving Beckmann rearrangement
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/36Oxygen or sulfur atoms
    • C07D207/382-Pyrrolones
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Hospice & Palliative Care (AREA)
  • Urology & Nephrology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrrole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

LA INVENCIÓN SE REFIERE A UN PROCESO PARA PRODUCIR INHIBIDORES DE NEP O PRO-FÁRMACOS<br /> DE LOS MISMOS, EN PARTICULAR INHIBIDORES DE NEP QUE COMPRENDEN UNA ESTRUCTURA BASE DE<br /> ÁCIDO Y-AMINO-Ó-BIFENIL-A-METIL-ALCANOICO, O DE UN ÉSTER DE ÁCIDO. CON DETALLE, LOS<br /> PROCESOS, DE ACUERDO CON LA PRESENTE INVENCION, SE RELACIONAN POR ÚLTIMO CON LA<br /> SÍNTESIS DE INTERMEDIARIOS PARA PREPARAR LOS INHIBIDORES DE NEP ANTERIORES, ES DECIR,<br /> LOS COMPUESTOS DE ACUERDO CON LA FÓRMULA (1), O UNA SAL DE LOS MISMOS QUE SE OBTIENE<br /> A PARTIR DE LA REDUCCIÓN DE UN COMPUESTO INTERMEDIARIO DE FÓRMULA (2) COMO SE MUESTRA<br /> A CONTINUACIÓN:<br /> EN DONDE R1 Y R2 SON, INDEPENDIENTEMENTE UNO DEL OTRO, HIDROGENO O UN GRUPO PROTECTOR DE NITROGENO,<br /> Y R3 ES UN GRUPO CARBOXILO O UN GRUPO ESTER, DE PREFERENCIA UN GRUPO CARBOXILO O ALQUIL-ESTER.<br /> COMPLEMENTARIAMENTE LA INVENCION SE REFIERE A LOS COMPUESTOS INTERMEDIARIOS DE DICHOS<br /> INHIBIDORES DE NEP ASI COMO A LA SINTESIS DE DICHOS COMPUESTOS INTERMEDIARIOS.<br />  THE INVENTION REFERS TO A PROCESS FOR PRODUCING NEP INHIBITORS OR PRO-DRUGS <br /> OF THE SAME, IN PARTICULAR NEP INHIBITORS THAT INCLUDE A BASE STRUCTURE OF <br /> ACID AND-AMINO-OR-BIPHENYL-A- METHYL-ALKANOIC, OR OF AN ACID ESTER. IN DETAIL, THE <br /> PROCESSES, IN ACCORDANCE WITH THE PRESENT INVENTION, LASTLY RELATE TO THE SYNTHESIS OF INTERMEDIARIES TO PREPARE THE ABOVE NEP INHIBITORS, THAT IS, <br /> THE COMPOUNDS IN ACCORDANCE WITH THE FORMULA (1), OR A SALT OF THE SAME THAT IS OBTAINED <br /> FROM THE REDUCTION OF AN INTERMEDIARY COMPOUND OF FORMULA (2) AS SHOWN <br /> BELOW: <br /> WHERE R1 AND R2 ARE, INDEPENDENTLY ONE OF THE OTHER, HYDROGEN OR A NITROGEN PROTECTIVE GROUP, <br /> AND R3 IS A CARBOXYL GROUP OR AN ESTER GROUP, PREFERABLY A CARBOXYL OR ALKYL-ESTER GROUP. <br /> COMPLEMENTARY TO THE INVENTION. REFERS TO THE INTERMEDIARY COMPOUNDS OF SUCH INTERMEDIARY <br /> NEP INHIBITORS AS WELL AS THE SYNTHESIS OF SUCH INTERMEDIARY COMPOUNDS. <br />

CL2009000089A 2008-01-17 2009-01-16 Processes for preparing a derivative of y-amino-o-biphenyl-x-methyl-pentanoic acid, intermediate compounds and their preparation process; use of the compounds in the synthesis of nep inhibitor compounds, useful in cardiovascular diseases, such as hypertension, congestive heart failure, among others. CL2009000089A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP08150353 2008-01-17

Publications (1)

Publication Number Publication Date
CL2009000089A1 true CL2009000089A1 (en) 2010-01-22

Family

ID=40758693

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2009000089A CL2009000089A1 (en) 2008-01-17 2009-01-16 Processes for preparing a derivative of y-amino-o-biphenyl-x-methyl-pentanoic acid, intermediate compounds and their preparation process; use of the compounds in the synthesis of nep inhibitor compounds, useful in cardiovascular diseases, such as hypertension, congestive heart failure, among others.

Country Status (29)

Country Link
US (4) US8580974B2 (en)
EP (1) EP2245009B1 (en)
JP (2) JP5739667B2 (en)
KR (1) KR101587668B1 (en)
CN (2) CN101952249B (en)
AR (1) AR070176A1 (en)
AU (1) AU2009204759B2 (en)
BR (1) BRPI0906764A2 (en)
CA (1) CA2711529C (en)
CL (1) CL2009000089A1 (en)
CO (1) CO6290677A2 (en)
EC (1) ECSP10010405A (en)
ES (1) ES2602564T3 (en)
GT (1) GT201000211A (en)
HU (1) HUE030606T2 (en)
IL (1) IL206664A0 (en)
MA (1) MA31951B1 (en)
MX (1) MX2010007842A (en)
MY (1) MY169425A (en)
NZ (2) NZ600119A (en)
PE (1) PE20091364A1 (en)
PL (1) PL2245009T3 (en)
PT (1) PT2245009T (en)
RU (2) RU2513521C2 (en)
SG (1) SG187491A1 (en)
SI (1) SI2245009T1 (en)
TN (1) TN2010000304A1 (en)
TW (1) TWI422370B (en)
WO (1) WO2009090251A2 (en)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR070176A1 (en) * 2008-01-17 2010-03-17 Novartis Ag SYNTHESIS PROCESSES OF NEP INHIBITORS, INTERMEDIATE COMPOUNDS AND USE OF THE SAME IN SYNTHESIS
US8450496B2 (en) * 2009-03-24 2013-05-28 Hoffman-La Roche Inc. Process for the preparation of propionic acid derivatives
AR076706A1 (en) 2009-05-28 2011-06-29 Novartis Ag AMINOBUTIRIC DERIVATIVES REPLACED AS NEPRILISINE INHIBITORS
MX2011012628A (en) 2009-05-28 2011-12-14 Novartis Ag Substituted aminopropionic derivatives as neprilysin inhibitors.
RU2534619C2 (en) 2009-09-23 2014-11-27 Чжэцзян Цзючжоу Фармасьютикл Ко., Лтд. Method of obtaining n-acylbiphenylalanine
JO2967B1 (en) 2009-11-20 2016-03-15 نوفارتس ايه جي Substituted carbamoylmethylamino acetic acid derivatives as novel NEP inhibitors
MX2012008483A (en) * 2010-01-22 2012-08-15 Novartis Ag Intermediates of neutral endopeptidase inhibitors and preparation method thereof.
AU2011295170B2 (en) 2010-08-23 2014-12-18 Novartis Ag Process for the preparation of intermediates for the manufacture of NEP inhibitors
ES2608780T3 (en) 2010-08-23 2017-04-17 Novartis Ag New process for the preparation of intermediaries useful for the preparation of NEP inhibitors
CN103080077B (en) * 2010-08-23 2015-06-10 诺华股份有限公司 Process for the preparation of intermediates for the manufacture of NEP inhibitors
US8673974B2 (en) 2010-11-16 2014-03-18 Novartis Ag Substituted amino bisphenyl pentanoic acid derivatives as NEP inhibitors
NZ611528A (en) 2010-12-15 2015-06-26 Theravance Biopharma R & D Ip Llc Neprilysin inhibitors
DK2651896T3 (en) 2010-12-15 2015-10-05 Theravance Biopharma R & D Ip Llc Neprilysininhibitorer
KR101854874B1 (en) 2011-02-17 2018-05-04 세라밴스 바이오파마 알앤디 아이피, 엘엘씨 Substituted aminobutyric derivatives as neprilysin inhibitors
WO2012154249A1 (en) 2011-02-17 2012-11-15 Theravance, Inc. Substituted aminobutyric derivatives as neprilysin inhibitors
JP5959075B2 (en) 2011-05-31 2016-08-02 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー Neprilysin inhibitor
CA2835216A1 (en) 2011-05-31 2012-12-06 Theravance, Inc. Neprilysin inhibitors
ES2642883T3 (en) 2011-05-31 2017-11-20 Theravance Biopharma R&D Ip, Llc Neprilysin inhibitors
TWI560172B (en) 2011-11-02 2016-12-01 Theravance Biopharma R&D Ip Llc Neprilysin inhibitors
WO2013181332A1 (en) 2012-05-31 2013-12-05 Theravance, Inc. Nitric oxide donor neprilysin inhibitors
ES2710932T3 (en) 2012-06-08 2019-04-29 Theravance Biopharma R&D Ip Llc Neprilysin inhibitors
SI2864292T1 (en) 2012-06-08 2017-07-31 Theravance Biopharma R&D Ip, Llc Neprilysin inhibitors
NZ704741A (en) 2012-08-08 2017-10-27 Theravance Biopharma R&D Ip Llc Neprilysin inhibitors
KR20150119107A (en) 2013-02-14 2015-10-23 노파르티스 아게 Substituted bisphenyl butanoic acid derivatives as nep inhibitors with improved in vivo efficacy
KR20150119109A (en) 2013-02-14 2015-10-23 노파르티스 아게 Substituted bisphenyl butanoic phosphonic acid derivatives as nep (neutral endopeptidase) inhibitors
ES2634218T3 (en) 2013-03-05 2017-09-27 Theravance Biopharma R&D Ip, Llc Neprilysin inhibitors
CN110590606B (en) * 2013-11-15 2023-02-17 豪夫迈·罗氏有限公司 Process for preparing pyrimidylcyclopentane compounds
MX2016009759A (en) 2014-01-30 2016-11-17 Theravance Biopharma R&D Ip Llc 5-biphenyl-4-heteroarylcarbonylamino-pentanoic acid derivatives as neprilysin inhibitors.
MX2016009760A (en) 2014-01-30 2016-11-08 Theravance Biopharma R&D Ip Llc Neprilysin inhibitors.
DK3218351T3 (en) 2014-11-14 2019-09-16 Zentiva Ks PROCEDURE FOR MANUFACTURING, INSULATING AND CLEANING PHARMACEUTICAL APPLICABLE FORMS OF AHU-377
ES2883557T3 (en) * 2014-12-19 2021-12-09 Basf Se Composition for use in a process for the preparation of optically active carbonyl compounds
JP6766055B2 (en) 2015-02-11 2020-10-07 セラヴァンス バイオファーマ アール&ディー アイピー, エルエルシー (2S, 4R) -5- (5'-chloro-2'-fluorobiphenyl-4-yl) -4- (ethoxyoxalylamino) -2-hydroxymethyl-2-methylpentanoic acid as a neprilysin inhibitor
TW201632493A (en) 2015-02-13 2016-09-16 諾華公司 New process
ES2857101T3 (en) 2015-02-19 2021-09-28 Theravance Biopharma R&D Ip Llc (2R,4R)-5-(5'-chloro-2'-fluorobiphenyl-4-yl)-2-hydroxy-4-[(5-methyloxazole-2-carbonyl)amino]pentanoic acid
CN106146351B (en) * 2015-04-03 2020-09-11 博瑞生物医药(苏州)股份有限公司 Method for producing biaryl substituted 4-amino-butyric acids or derivatives thereof
CN105061263B (en) * 2015-08-11 2017-03-15 苏州楚凯药业有限公司 A kind of preparation method of nep inhibitor intermediate
CN105152980B (en) * 2015-09-11 2017-03-29 浙江永宁药业股份有限公司 N tertbutyloxycarbonyls(4S)‑(To phenylphenylmethyl)4 amino(2R)The chiral method for preparing of methylbutanoic acid
WO2017051326A1 (en) 2015-09-23 2017-03-30 Novartis Ag New processes and intermediates useful in synthesis of nep inhibitors
RU2769445C2 (en) 2015-12-10 2022-03-31 Новартис Аг New method and new intermediate compounds
BR112018011788A2 (en) 2015-12-11 2018-12-04 Zentiva Ks (2r, 4s) -5- (biphenyl-4-yl) -4 - [(3-carboxypropionyl) amino] -2-methylpentanoic acid ethyl ester solid forms, their salts and a preparation method
PT3408260T (en) 2016-03-08 2021-07-23 Theravance Biopharma R&D Ip Llc Crystalline(2s,4r)-5-(5'-chloro-2'-fluoro-[1,1'-biphenyl]-4-yl)-2-(ethoxymethyl)-4-(3-hydroxyisoxazole-5-carboxamido)-2-methylpentanoic acid and uses thereof
JP6944473B2 (en) 2016-07-05 2021-10-06 ノバルティス アーゲー A new method for early sacubitril intermediates
EP3500549B1 (en) 2016-08-17 2020-12-16 Novartis AG New processes and intermediates for nep inhibitor synthesis
CN110088079A (en) 2016-12-23 2019-08-02 诺华股份有限公司 New method for early stage husky card cloth song intermediate
EP3421455B1 (en) * 2017-06-29 2019-03-27 F.I.S.- Fabbrica Italiana Sintetici S.p.A. Improved process for the preparation of chiral 3-amino-piperidins, useful intermediates for the preparation of tofacitinib
CN109912508B (en) * 2019-04-30 2022-08-12 上海天慈国际药业有限公司 Preparation method of dexmedetomidine and hydrochloride thereof
CN110878039A (en) * 2019-12-18 2020-03-13 株洲千金药业股份有限公司 Preparation method of Sacubitril valsartan sodium impurity
CN115611857B (en) * 2022-09-09 2024-05-31 上海伍夫科技有限公司 Preparation method of 2-methyl-5- (1-methylpyrrolidine-2-yl) pyridine
CN115772088A (en) * 2022-12-28 2023-03-10 海门瑞一医药科技有限公司 Preparation method of tert-butoxy (bisdimethylamino) methane

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0055175B1 (en) 1980-12-23 1984-06-13 Air Industrie Thermo-electrical plants
US5250552A (en) 1991-05-09 1993-10-05 Warner-Lambert Company 3-[thiazolidinone, oxazolidinone, imidazolidinone]-indoles as antiinflammatory agents
US5250522A (en) 1992-10-09 1993-10-05 Ciba-Geigy Corporation Phosphono/biaryl substituted amino acid derivatives
FR2688503B1 (en) 1992-03-16 1994-05-06 Synthelabo PROCESS FOR THE PREPARATION OF 2- (TETRAZOL-5-YL) - [1,1'-BIPHENYL] DERIVATIVES.
EP0550313A1 (en) 1991-12-30 1993-07-07 Synthelabo 2-(Tetranol-5-yl)-(1,1'-biphenyl)derivatives, their preparation and use as intermediates
US5217996A (en) * 1992-01-22 1993-06-08 Ciba-Geigy Corporation Biaryl substituted 4-amino-butyric acid amides
US5412102A (en) 1994-05-27 1995-05-02 Syntex (U.S.A.) Inc. Processes for preparing 1-butyl-2-[2'-(2H-tetrazol-5-yl) biphenyl-4-ylmethyl]-1H-indole-3-carboxylic acid
TW536540B (en) * 1997-01-30 2003-06-11 Bristol Myers Squibb Co Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe
GB0402262D0 (en) 2004-02-02 2004-03-10 Novartis Ag Process for the manufacture of organic compounds
AR057882A1 (en) * 2005-11-09 2007-12-26 Novartis Ag DOUBLE ACTION COMPOUNDS OF ANGIOTENSIN RECEPTOR BLOCKERS AND NEUTRAL ENDOPEPTIDASE INHIBITORS
EP1903027A1 (en) * 2006-09-13 2008-03-26 Novartis AG Process for preparing biaryl substituted 4-amino-butyric acid or derivatives thereof and their use in the production of NEP inhibitors
BRPI0806700A8 (en) * 2007-01-12 2019-01-22 Novartis Ag process
EP2532673A3 (en) 2007-05-10 2014-01-08 R & D Biopharmaceuticals Gmbh Tubulysine derivatives
AR070176A1 (en) * 2008-01-17 2010-03-17 Novartis Ag SYNTHESIS PROCESSES OF NEP INHIBITORS, INTERMEDIATE COMPOUNDS AND USE OF THE SAME IN SYNTHESIS
MX2012008483A (en) * 2010-01-22 2012-08-15 Novartis Ag Intermediates of neutral endopeptidase inhibitors and preparation method thereof.
ES2608780T3 (en) * 2010-08-23 2017-04-17 Novartis Ag New process for the preparation of intermediaries useful for the preparation of NEP inhibitors
AU2011295170B2 (en) * 2010-08-23 2014-12-18 Novartis Ag Process for the preparation of intermediates for the manufacture of NEP inhibitors

Also Published As

Publication number Publication date
TW200938188A (en) 2009-09-16
US9403766B2 (en) 2016-08-02
MX2010007842A (en) 2010-08-09
US20140243546A1 (en) 2014-08-28
US20110046397A1 (en) 2011-02-24
BRPI0906764A2 (en) 2015-08-18
WO2009090251A2 (en) 2009-07-23
JP5800882B2 (en) 2015-10-28
US9061973B2 (en) 2015-06-23
GT201000211A (en) 2014-03-14
AR070176A1 (en) 2010-03-17
CN101952249B (en) 2013-10-16
RU2010133903A (en) 2012-02-27
MA31951B1 (en) 2010-12-01
TN2010000304A1 (en) 2011-11-11
ES2602564T3 (en) 2017-02-21
RU2513521C2 (en) 2014-04-20
MY169425A (en) 2019-04-04
IL206664A0 (en) 2010-12-30
US8580974B2 (en) 2013-11-12
CN103483236B (en) 2016-09-28
ECSP10010405A (en) 2010-09-30
NZ586657A (en) 2012-06-29
PE20091364A1 (en) 2009-10-13
SG187491A1 (en) 2013-02-28
CN103483236A (en) 2014-01-01
CO6290677A2 (en) 2011-06-20
EP2245009B1 (en) 2016-08-10
CN101952249A (en) 2011-01-19
HUE030606T2 (en) 2017-05-29
RU2636936C2 (en) 2017-11-29
SI2245009T1 (en) 2016-12-30
PL2245009T3 (en) 2017-06-30
AU2009204759B2 (en) 2012-06-07
KR101587668B1 (en) 2016-01-22
US20160060217A1 (en) 2016-03-03
EP2245009A2 (en) 2010-11-03
RU2013148670A (en) 2015-05-10
TWI422370B (en) 2014-01-11
NZ600119A (en) 2013-07-26
PT2245009T (en) 2016-11-10
KR20100119867A (en) 2010-11-11
JP2011510097A (en) 2011-03-31
AU2009204759A1 (en) 2009-07-23
CA2711529A1 (en) 2009-07-23
WO2009090251A3 (en) 2009-12-23
JP2014070076A (en) 2014-04-21
US9227934B2 (en) 2016-01-05
CA2711529C (en) 2016-11-22
JP5739667B2 (en) 2015-06-24
US20150246881A1 (en) 2015-09-03

Similar Documents

Publication Publication Date Title
CL2009000089A1 (en) Processes for preparing a derivative of y-amino-o-biphenyl-x-methyl-pentanoic acid, intermediate compounds and their preparation process; use of the compounds in the synthesis of nep inhibitor compounds, useful in cardiovascular diseases, such as hypertension, congestive heart failure, among others.
CO6400217A2 (en) (1-PHENYL-2-PIRIDIN-4-IL) ETHYL ESTERS OF BENZOIC ACID AS PHOSPHODIESTERASE INHIBITORS
UY32142A (en) PREPARATION OF A QUINOLINILOXIDIFENILCICLOPROPANODICARBOXAMIDA
EA201270550A1 (en) PROCESS FOR OBTAINING COMPOUNDS FOR APPLICATION AS SGLT2 INHIBITORS
UY31367A1 (en) DERIVATIVES OF NICOTINAMIDE, ITS PREPARATION AND ITS APPLICATION IN THERAPEUTICS
MA31574B1 (en) PYRAZOLE DERIVATIVES AND THEIR USE AS INHIBITORS OF RAF
CR20110013A (en) Heteroaryl Derivatives as DGAT1 Inhibitors
CO6290658A2 (en) DERIVATIVES OF AZETIDINE AND CYCLLOBUTANE AS JACK INHIBITORS
AR074845A1 (en) SYNTHESIS PROCEDURE OF IVABRADINE AND ITS ADDITION SALTS TO A PHARMACEUTICALLY ACCEPTABLE ACID
IN2014MN01521A (en)
MA31080B1 (en) CYCLED DERIVATIVES AS EG-5 INHIBITORS.
CY1115623T1 (en) METHOD FOR COMPOSITION OF 7,8-DIMETHOXY-1,3-DIDHYRO-2H-3-BENZAZEPIN-2-ONE AND ITS APPLICATION TO THE SYNTHESIS OF IBABRADYN AS
AU2009310099A8 (en) Agricultural compositions
NI201000049A (en) METHOD TO PRODUCE 2&#39;-DEOXY-5-AZACITIDINE (DECITABIN)
ES2721662T3 (en) Process for the preparation of travoprost
PT2462098E (en) Process for the preparation of derivatives of 1-(2-halobiphenyl-4-yl)-cyclopropanecarboxylic acid
UY33179A (en) CARBOXYL ACID DERIVATIVES THAT INCLUDE A 2,5-REPLACED OXAZOLOPIRIMIDINE RING.
MX2010009926A (en) New process for the preparatiion of cyclohexanecarboxylic acid dericatives.
BR112013015532B1 (en) 2- (alkoxy or aryloxycarbonyl) -4-methyl-6- (2,6,6-trimethylcycloex-1-enyl) -hex-2-enoic acid, method for its preparation and uses
EA201592167A1 (en) METHOD FOR OBTAINING DERIVATIVES OF PYRROLIDIN-2-CARBONIC ACID
UA113223C2 (en) ARYLETINYLPYRIMIDINE
UY33507A (en) PROCESS FOR THE PREPARATION OF ENOLATE SALTS OF 4-FLUORO-2-HYDROXIMETHYLENE-3-OXO-BUTIRATES
JO2851B1 (en) Substituted 3-Benzofuranyl-Indol-2-One-3-Acetamidopiperazine Derivatives, Preparation Thereof And Therapeutic Application Thereof
WO2012052939A3 (en) Preparation of bicyclo[2.2.2]octan-2-one compounds
MX2013004425A (en) Diastereoselective preparation of bicyclo[2.2.2]octan-2-one compounds.